SCHEMBL30432465

SCHEMBL30432465

CC[C@H](C)[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CS)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC(C)C)C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@H](C(=O)N1CCC[C@H]1C(=O)NCC(=O)NCC(=O)O)C(C)C

nearest known ligand 0.63

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ CALCR P30988 6/20 0.63
▸ F2 P00734 4/20 0.57
▸ CRHR1 P34998 1/20 0.56
▸ CRHR2 Q13324 1/20 0.56
▸ HCRTR1 O43613 1/20 0.56
▸ HCRTR2 O43614 1/20 0.56
▸ CXCR4 P61073 1/20 0.55
▸ CCKBR P32239 2/20 0.53
▸ GLP1R P43220 2/20 0.53
▸ NPY2R P49146 2/20 0.51
▸ NPY4R P50391 2/20 0.51
▸ NPY5R Q15761 2/20 0.51
▸ NPY1R P25929 1/20 0.51

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL30432386 0.90 F2 (0.62) CALCRF2CRHR1CRHR2HCRTR1
SCHEMBL31182855 0.89 CALCR (0.65) CALCRF2CRHR1CRHR2HCRTR1
SCHEMBL31014074 0.88 CALCR (0.75) CALCRF2CRHR1CRHR2HCRTR1
SCHEMBL30431826 0.88 CALCR (0.59) CALCRF2CRHR1CRHR2HCRTR1
SCHEMBL31182742 0.88 CALCR (0.61) CALCRF2CRHR1CRHR2HCRTR1
SCHEMBL30433583 0.87 CALCR (0.64) CALCRF2HCRTR1HCRTR2CXCR4
SCHEMBL30431873 0.87 CALCR (0.70) CALCRF2CRHR1CRHR2HCRTR1
SCHEMBL31000925 0.86 CALCR (0.76) CALCRF2CRHR1CRHR2HCRTR1
SCHEMBL30431750 0.86 F2 (0.70) CALCRF2CRHR1CRHR2HCRTR1
SCHEMBL29961384 0.86 CALCR (0.63) CALCRF2CRHR1CRHR2HCRTR1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240342111-A1 ISOMER-SPECIFIC NEUROPROTECTIVE EFFECT OF NATURAL RESERVATROL UNIV SOUTH CAROLINA (US) 2024-10-17 — — US disclosed
US-20230201133-A1 Isomer-Specific Neuroprotective Effect of Natural Resveratrol UNIVERSITY OF SOUTH CAROLINA (US) 2023-06-29 — — US disclosed
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